Issue 15, 2019

Radical fluoroalkylation reactions of (hetero)arenes and sulfides under red light photocatalysis

Abstract

Fluoroalkylation reactions of (hetero)aromatics have been accomplished through the low-power illumination from red LEDs (λmax = 635 nm) of commercially available perfluoroalkyl iodides RF-I and phthalocyanine zinc salt as photocatalyst in MeCN : DMF solvent mixture. This methodology has been extended to the perfluorobutylation of sulfides. As far as we are concerned, this is the first report on a perfluoroalkylation reaction of (hetero)aromatics and sulfides under red-light photocatalysis.

Graphical abstract: Radical fluoroalkylation reactions of (hetero)arenes and sulfides under red light photocatalysis

Supplementary files

Article information

Article type
Communication
Submitted
27 Feb 2019
Accepted
22 Mar 2019
First published
25 Mar 2019

Org. Biomol. Chem., 2019,17, 3741-3746

Radical fluoroalkylation reactions of (hetero)arenes and sulfides under red light photocatalysis

D. E. Yerien, M. V. Cooke, M. C. García Vior, S. Barata-Vallejo and A. Postigo, Org. Biomol. Chem., 2019, 17, 3741 DOI: 10.1039/C9OB00486F

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements